| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:128153383-128153514 | Rare:42 | ||||
| chr3:128650567-128650884 | Common:2; Rare:140 | ||||
| chr3:128680633-128680883 | Common:3; Rare:76 | ||||
| chr3:128879425-128879880 | Common:4; Rare:210; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
| chr3:129183764-129184079 | Common:2; Rare:105 | ||||
| chr3:129249525-129249683 | Common:2; Rare:49 | ||||
| chr3:129278777-129278899 | Common:3; Rare:33 | ||||
| chr3:129315861-129316360 | Common:5; Rare:179 | ||||
| chr3:129439824-129440383 | Common:1; Rare:168; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:129893539-129893882 | Rare:134 | ||||
| chr3:130850508-130850717 | Common:1; Rare:37 | ||||
| chr3:130893911-130894237 | Common:3; Rare:93 | ||||
| chr3:130993834-130994013 | Rare:45; Clinvar:1 | ||||
| chr3:131026716-131026940 | Common:2; Rare:56 | ||||
| chr3:131381479-131381811 | Common:2; Rare:84 |